Linked Data
ClinVar Variation Id:
50181
dbSNP Id:
rs45517162
ExAC:
16:2112533 G / A
gnomAD v2:
16-2112533-G-A
gnomAD v3:
16-2062532-G-A
gnomAD v4:
16-2062532-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2062532G>A , CM000678.2:g.2062532G>A | GRCh38 |
| NC_000016.9:g.2112533G>A , CM000678.1:g.2112533G>A | GRCh37 |
| NC_000016.8:g.2052534G>A | NCBI36 |
| NG_005895.1:g.18227G>A , LRG_487:g.18227G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.1293G>A | ENSP00000455997.2:p.Ala431= | |
| ENST00000642206.2:c.1338G>A | ENSP00000495146.2:p.Ala446= | |
| ENST00000642365.2:c.1293G>A | ENSP00000495459.2:p.Ala431= | |
| ENST00000644417.2:c.*730G>A | ENSP00000493912.2:n.*730G>A | |
| ENST00000646464.2:c.*898G>A | ENSP00000496610.2:n.*898G>A | |
| ENST00000219476.9:c.1293G>A MANE Select | ENSP00000219476.3:p.Ala431= | |
| ENST00000350773.9:c.1293G>A | ENSP00000344383.4:p.Ala431= | |
| ENST00000401874.7:c.1293G>A | ENSP00000384468.2:p.Ala431= | |
| ENST00000463601.2:n.203G>A | ||
| ENST00000467949.2:n.463G>A | ||
| ENST00000568454.6:c.1326G>A | ENSP00000454487.1:p.Ala442= | |
| ENST00000642561.1:c.1293G>A | ENSP00000495099.1:p.Ala431= | |
| ENST00000642797.1:c.1293G>A | ENSP00000493846.1:p.Ala431= | |
| ENST00000642812.1:n.1338G>A | ||
| ENST00000642936.1:c.1293G>A | ENSP00000494514.1:p.Ala431= | |
| ENST00000643088.1:c.1293G>A | ENSP00000494747.1:p.Ala431= | |
| ENST00000643149.1:n.3303G>A | ||
| ENST00000643298.1:c.*795G>A | ENSP00000494393.1:n.*795G>A | |
| ENST00000643745.1:c.*225G>A | ENSP00000495948.1:n.*225G>A | |
| ENST00000643946.1:c.1293G>A | ENSP00000495927.1:p.Ala431= | |
| ENST00000644043.1:c.1293G>A | ENSP00000496262.1:p.Ala431= | |
| ENST00000644135.1:c.1293G>A | ENSP00000495644.1:p.Ala431= | |
| ENST00000644222.1:n.1380G>A | ||
| ENST00000644329.1:c.1293G>A | ENSP00000496611.1:p.Ala431= | |
| ENST00000644335.1:c.1293G>A | ENSP00000496317.1:p.Ala431= | |
| ENST00000644399.1:c.1286G>A | ||
| ENST00000644665.1:n.2467G>A | ||
| ENST00000644847.1:n.285G>A | ||
| ENST00000645591.1:n.2351G>A | ||
| ENST00000646388.1:c.1293G>A | ENSP00000495921.1:p.Ala431= | |
| ENST00000646634.1:n.306G>A | ||
| ENST00000647234.1:n.3051G>A | ||
| ENST00000647242.1:n.1929G>A | ||
| ENST00000219476.7:c.1293G>A | ENSP00000219476.3:p.Ala431= | |
| ENST00000350773.8:c.1293G>A | ENSP00000344383.4:p.Ala431= | |
| ENST00000382538.10:c.1146G>A | ENSP00000371978.6:p.Ala382= | |
| ENST00000401874.6:c.1293G>A | ENSP00000384468.2:p.Ala431= | |
| ENST00000439117.6:c.*592G>A | ENSP00000406980.2:n.*592G>A | |
| ENST00000439673.6:c.1182G>A | ENSP00000399232.2:p.Ala394= | |
| ENST00000463601.1:n.456G>A | ||
| ENST00000467949.1:c.447G>A | ENSP00000454997.1:p.Ala149= | |
| ENST00000568454.5:c.1326G>A | ENSP00000454487.1:p.Ala442= | |
| ENST00000568566.5:c.15G>A | ENSP00000455997.1:p.Ala5= | |
| NM_000548.3:c.1293G>A , LRG_487t1:c.1293G>A | NP_000539.2:p.Ala431= | |
| NM_001077183.1:c.1293G>A | NP_001070651.1:p.Ala431= | |
| NM_001114382.1:c.1293G>A | NP_001107854.1:p.Ala431= | |
| XM_005255529.3:c.1293G>A | XP_005255586.2:p.Ala431= | |
| XM_005255531.3:c.1293G>A | XP_005255588.2:p.Ala431= | |
| XM_011522636.1:c.1293G>A | XP_011520938.1:p.Ala431= | |
| XM_011522637.1:c.1293G>A | XP_011520939.1:p.Ala431= | |
| XM_011522638.1:c.1182G>A | XP_011520940.1:p.Ala394= | |
| XM_011522639.1:c.1293G>A | XP_011520941.1:p.Ala431= | |
| XM_011522640.1:c.1293G>A | XP_011520942.1:p.Ala431= | |
| XM_011522641.1:c.1182G>A | XP_011520943.1:p.Ala394= | |
| NM_000548.4:c.1293G>A | NP_000539.2:p.Ala431= | |
| NM_001077183.2:c.1293G>A | NP_001070651.1:p.Ala431= | |
| NM_001114382.2:c.1293G>A | NP_001107854.1:p.Ala431= | |
| NM_001318827.1:c.1182G>A | NP_001305756.1:p.Ala394= | |
| NM_001318829.1:c.1146G>A | NP_001305758.1:p.Ala382= | |
| NM_001318831.1:c.693G>A | NP_001305760.1:p.Ala231= | |
| NM_001318832.1:c.1326G>A | NP_001305761.1:p.Ala442= | |
| NM_001363528.1:c.1293G>A | NP_001350457.1:p.Ala431= | |
| NM_021055.2:c.1293G>A | NP_066399.2:p.Ala431= | |
| XM_005255531.4:c.1293G>A | XP_005255588.2:p.Ala431= | |
| XM_011522636.2:c.1293G>A | XP_011520938.1:p.Ala431= | |
| XM_011522637.2:c.1293G>A | XP_011520939.1:p.Ala431= | |
| XM_011522638.2:c.1455G>A | XP_011520940.2:p.Ala485= | |
| XM_011522639.2:c.1293G>A | XP_011520941.1:p.Ala431= | |
| XM_011522640.2:c.1293G>A | XP_011520942.1:p.Ala431= | |
| XM_017023615.1:c.1293G>A | XP_016879104.1:p.Ala431= | |
| XM_017023616.1:c.1293G>A | XP_016879105.1:p.Ala431= | |
| XM_017023617.1:c.1455G>A | XP_016879106.1:p.Ala485= | |
| XM_017023618.1:c.-52G>A | XP_016879107.1:n.-52G>A | |
| XM_024450413.1:c.1293G>A | XP_024306181.1:p.Ala431= | |
| NM_000548.5:c.1293G>A MANE Select | NP_000539.2:p.Ala431= | |
| NM_001370404.1:c.1293G>A | NP_001357333.1:p.Ala431= | |
| NM_001370405.1:c.1293G>A | NP_001357334.1:p.Ala431= | |
| NM_001077183.3:c.1293G>A | NP_001070651.1:p.Ala431= | |
| NM_001114382.3:c.1293G>A | NP_001107854.1:p.Ala431= | |
| NM_001318827.2:c.1182G>A | NP_001305756.1:p.Ala394= | |
| NM_001318829.2:c.1146G>A | NP_001305758.1:p.Ala382= | |
| NM_001318831.2:c.693G>A | NP_001305760.1:p.Ala231= | |
| NM_001318832.2:c.1326G>A | NP_001305761.1:p.Ala442= | |
| NM_001363528.2:c.1293G>A | NP_001350457.1:p.Ala431= | |
| NM_021055.3:c.1293G>A | NP_066399.2:p.Ala431= |